Department of Respiratory Medicine, Alfred Health, Melbourne, Victoria, Australia.
Department of Respiratory and Sleep Medicine, Eastern Health, Melbourne, Victoria, Australia.
Respirology. 2024 Sep;29(9):795-802. doi: 10.1111/resp.14763. Epub 2024 Jun 2.
Evidence for the benefit of steroid therapy in acute exacerbations (AEs) of idiopathic pulmonary fibrosis (IPF) is limited; however, they remain a cornerstone of management in other fibrotic interstitial lung diseases. This retrospective observational study assesses the effect of steroid treatment on in-hospital mortality in patients with acute exacerbation of fibrotic interstitial lung disease (AE-FILD) including IPF and non-IPF ILDs.
AE-FILD cases over a 10-year period were filtered using a code-based algorithm followed by individual case evaluation. Binary logistic regression analysis was used to assess the relationship between corticosteroid treatment (defined as ≥0.5 mg/kg/day of prednisolone-equivalent for ≥3 days within the first 72 h of admission) and in-hospital mortality or need for lung transplantation. Secondary outcomes included readmission, overall survival, requirement for domiciliary oxygen and rehabilitation.
Across two centres a total of 107 AE-FILD subjects were included, of which 46 patients (43%) received acute steroid treatment. The steroid cohort was of younger age with fewer comorbidities but had higher oxygen requirements. Pre-admission FVC and DLCO, distribution of diagnoses and smoking history were similar. The mean steroid treatment dose was 4.59 mg/kg/day. Steroid use appeared to be associated with increased risk of inpatient mortality or transplantation (OR 4.11; 95% CI 1.00-16.83; p = 0.049). In the steroid group, there appeared to be a reduced risk of all-cause mortality in non-IPF patients (HR 0.21; 95% CI 0.04-0.96; p = 0.04) compared to their IPF counterparts. Median survival was reduced in the steroid group (221 vs. 520.5 days) with increased risk of all-cause mortality (HR 3.25; 95% CI 1.56-6.77; p < 0.01).
In this two-centre retrospective study of 107 patients, AE-FILD demonstrates a high risk of mortality, at a level similar to that seen for AE-IPF, despite steroid treatment. Clinicians should consider other precipitating factors for exacerbations and use steroids judiciously. Further prospective trials are needed to determine the role of corticosteroids in AE-FILD.
类固醇治疗对特发性肺纤维化(IPF)急性加重(AE)的益处证据有限;然而,它们仍然是其他纤维性间质性肺疾病管理的基石。这项回顾性观察研究评估了类固醇治疗对包括 IPF 和非 IPFILD 在内的纤维性间质性肺疾病急性加重(AE-FILD)患者住院死亡率的影响。
使用基于代码的算法筛选了 10 年来的 AE-FILD 病例,然后进行了个体病例评估。使用二元逻辑回归分析评估皮质类固醇治疗(定义为入院前 72 小时内每天≥0.5mg/kg 泼尼松等效剂量≥3 天)与住院死亡率或肺移植的关系。次要结局包括再入院、总生存率、家庭氧疗和康复需求。
在两个中心共纳入了 107 例 AE-FILD 患者,其中 46 例(43%)接受了急性类固醇治疗。类固醇组年龄较小,合并症较少,但氧需求较高。入院前 FVC 和 DLCO、诊断分布和吸烟史相似。平均类固醇治疗剂量为 4.59mg/kg/天。类固醇的使用似乎与住院死亡率或移植风险增加相关(OR 4.11;95%CI 1.00-16.83;p=0.049)。在类固醇组中,与 IPF 患者相比,非 IPF 患者的全因死亡率似乎降低(HR 0.21;95%CI 0.04-0.96;p=0.04)。与非类固醇组相比,类固醇组的中位生存期缩短(221 与 520.5 天),全因死亡率增加(HR 3.25;95%CI 1.56-6.77;p<0.01)。
在这项对 107 例患者的两中心回顾性研究中,AE-FILD 显示出高死亡率风险,与 AE-IPF 相似,尽管进行了类固醇治疗。临床医生应考虑其他加重的诱发因素,并谨慎使用类固醇。需要进一步的前瞻性试验来确定皮质类固醇在 AE-FILD 中的作用。